先天性和非先天性色素沉着。

Modern problems in paediatrics Pub Date : 1976-10-20
Y Mishima
{"title":"先天性和非先天性色素沉着。","authors":"Y Mishima","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The hypofunction of melanocytes results in congenital and noncongenital depigmentation. Congenital depigmentation can be further divided into two groups; the first is depigmentation caused by loss of melanization in premelanosomes represented by oculocutaneous albinism; the second group is congenital decrease of melanocytes represented by nevus dipigmentosus. In contrast, acquired progressive depigmentation represented by vitiligo vulgaris and Sutton's leukoderma is characterized by the loss of premelanosome synthesis. The pathogenesis of these three major types of melanogenic defects has been further discussed with the current clinical, biological and immunological view of melanogenesis.</p>","PeriodicalId":76171,"journal":{"name":"Modern problems in paediatrics","volume":"20 ","pages":"18-37"},"PeriodicalIF":0.0000,"publicationDate":"1976-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Congenital and non-congenital depigmentation.\",\"authors\":\"Y Mishima\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The hypofunction of melanocytes results in congenital and noncongenital depigmentation. Congenital depigmentation can be further divided into two groups; the first is depigmentation caused by loss of melanization in premelanosomes represented by oculocutaneous albinism; the second group is congenital decrease of melanocytes represented by nevus dipigmentosus. In contrast, acquired progressive depigmentation represented by vitiligo vulgaris and Sutton's leukoderma is characterized by the loss of premelanosome synthesis. The pathogenesis of these three major types of melanogenic defects has been further discussed with the current clinical, biological and immunological view of melanogenesis.</p>\",\"PeriodicalId\":76171,\"journal\":{\"name\":\"Modern problems in paediatrics\",\"volume\":\"20 \",\"pages\":\"18-37\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1976-10-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Modern problems in paediatrics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Modern problems in paediatrics","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

黑色素细胞功能低下导致先天性和非先天性色素沉着。先天性色素沉着可进一步分为两类;第一种是由黑色素前体黑色素化丧失引起的色素脱失,以眼皮肤白化病为代表;第二组为先天性黑色素细胞减少,以色素沉着痣为代表。相反,以寻常白癜风和萨顿白皮病为代表的后天性进行性色素沉着以黑色素原体合成丧失为特征。这三种主要类型的黑素缺陷的发病机制已进一步讨论了目前的临床,生物学和免疫学观点的黑素发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Congenital and non-congenital depigmentation.

The hypofunction of melanocytes results in congenital and noncongenital depigmentation. Congenital depigmentation can be further divided into two groups; the first is depigmentation caused by loss of melanization in premelanosomes represented by oculocutaneous albinism; the second group is congenital decrease of melanocytes represented by nevus dipigmentosus. In contrast, acquired progressive depigmentation represented by vitiligo vulgaris and Sutton's leukoderma is characterized by the loss of premelanosome synthesis. The pathogenesis of these three major types of melanogenic defects has been further discussed with the current clinical, biological and immunological view of melanogenesis.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信